List the absolute stereochemistry at carbons 1,2,4 and five The image shows the chemical structure of brevisamide. Below is an explanation of the structure:**Chemical Structure Details:**1. **Molecular Framework:** - Brevisamide has a cyclic backbone and contains a six-membered ring. - The structure prominently features both double and single bonds.2. **Functional Groups:** - There is a hydroxyl group (OH) attached to carbon 4. - An amide group is present, where the nitrogen is connected to the carbon chain and a carbonyl group (C=O) with a methyl group (CH₃).3. **Numbering:** - The carbons in the central ring are numbered 1 through 5 for clarity. - This helps identify where different groups are attached.4. **Stereochemistry:** - The structure includes wedges and dashes indicating stereochemistry at carbons 4 and 5, illustrating the 3D orientation of the bonds. 5. **Side Chain:** - There is an extended side chain with several methyl groups (CH₃) and a double bond with a terminal carbonyl group featuring an aldehyde hydrogen (H).This compound can be studied for its potential biochemical or pharmaceutical applications.

Answered: Image /qna-images/answer/aae17f88-01b5-455c-9c81-96d90de38d35.jpg

Answered: H3C 2 HO CH3 CH3 H. CH3 brevisamide O:

Science

Chemistry

H3C 2 HO CH3 CH3 H. CH3 brevisamide O:

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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